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Sensory neurite outgrowth on white matter astrocytes is influenced by intracellular and extracellular S100A4 protein
Journal of neuroscience research, 2006-03, Vol.83 (4), p.619-626
Fang, Z.
Forslund, N.
Takenaga, K.
Lukanidin, E.
Kozlova, E.N.
2006
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Fang, Z.
Forslund, N.
Takenaga, K.
Lukanidin, E.
Kozlova, E.N.
Titel
Sensory neurite outgrowth on white matter astrocytes is influenced by intracellular and extracellular S100A4 protein
Ist Teil von
Journal of neuroscience research, 2006-03, Vol.83 (4), p.619-626
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2006
Quelle
MEDLINE
Beschreibungen/Notizen
The central nervous system (CNS) is considered a nonpermissive environment for axonal regeneration because of the presence of myelin and associated repulsive molecules. However, neural cells transplanted to the CNS preferably migrate and extend their fibers in white matter areas. We previously showed that white matter astrocytes in vivo express the calcium‐binding protein S100A4, which is strongly up‐regulated in areas of white matter degeneration. To investigate the role of white matter astrocytes and their specific protein S100A4 in axonal regeneration, we developed white matter astrocyte cultures with strong S100A4 expression and grew dissociated adult dorsal root ganglion (DRG) cells on top of astrocytes for 24 hr. By using small interfering S100A4 RNA, we were able to eliminate S100A4 expression and compare growth of DRG cell neurites on S100A4‐silenced and S100A4‐expressing astrocytes. In addition, we studied whether extracellular S100A4 has an effect on neurite growth from adult DRG cells cultured on S100A4‐expressing white matter astrocytes. Our data show that white matter astrocytes are permissive for neurite growth, although high levels of S100A4 in white matter astrocytes have a negative effect on this growth. Extracellular application of S100A4 induced extensive growth of DRG cell neurites on white matter astrocytes. These findings suggest that white matter astrocytes are able to support axonal regeneration and, furthermore, that administration of extracellular S100A4 provides strong additional support for axonal regeneration. © 2006 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0360-4012
eISSN: 1097-4547
DOI: 10.1002/jnr.20743
Titel-ID: cdi_swepub_primary_oai_DiVA_org_uu_22832
Format
–
Schlagworte
Animals
,
Astrocytes - physiology
,
calcium-binding protein
,
Cells, Cultured
,
dorsal root ganglion
,
Extracellular Space - metabolism
,
Ganglia, Spinal - cytology
,
Immunoblotting
,
Immunohistochemistry
,
in vitro
,
Intracellular Fluid - metabolism
,
nerve regeneration
,
Neurites - physiology
,
Neurons, Afferent - physiology
,
Polylysine - pharmacology
,
Rats
,
RNA, Small Interfering - genetics
,
S100 Calcium-Binding Protein A4
,
S100 Proteins - metabolism
,
S100 Proteins - physiology
,
S100 Proteins/metabolism/physiology
,
siRNA
,
Transfection
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